Abstract

A close to native structure of bulk biological specimens can be imaged by cryo-electron microscopy of vitreous sections (CEMOVIS). In some cases structural information can be combined with X-ray data leading to atomic resolution in situ. However, CEMOVIS is not routinely used. The two critical steps consist of producing a frozen section ribbon of a few millimeters in length and transferring the ribbon onto an electron microscopy grid. During these steps, the first sections of the ribbon are wrapped around an eyelash (unwrapping is frequent). When a ribbon is sufficiently attached to the eyelash, the operator must guide the nascent ribbon. Steady hands are required. Shaking or overstretching may break the ribbon. In turn, the ribbon immediately wraps around itself or flies away and thereby becomes unusable. Micromanipulators for eyelashes and grids as well as ionizers to attach section ribbons to grids were proposed. The rate of successful ribbon collection, however, remained low for most operators. Here we present a setup composed of two micromanipulators. One of the micromanipulators guides an electrically conductive fiber to which the ribbon sticks with unprecedented efficiency in comparison to a not conductive eyelash. The second micromanipulator positions the grid beneath the newly formed section ribbon and with the help of an ionizer the ribbon is attached to the grid. Although manipulations are greatly facilitated, sectioning artifacts remain but the likelihood to investigate high quality sections is significantly increased due to the large number of sections that can be produced with the reported tool.

Highlights

  • Biological structures close to their native state are best resolved in cryo-electron microscopy

  • Bulk samples are investigated by cryo-electron microscopy of vitreous sections (CEMOVIS) (Cryo-Electron Microscopy Of Vitreous Sections)

  • First attempts to produce cryosections were published by Fernandez-Moran and Dahl, (1952) and many others, but water was crystalline and for about 20 years the sections were dried before electron microscopy (EM) observation, which both lead to severe artifacts

Read more

Summary

Introduction

Biological structures close to their native state are best resolved in cryo-electron microscopy. Bulk samples are investigated by CEMOVIS (Cryo-Electron Microscopy Of Vitreous Sections). With both approaches the structures are fully hydrated and depicted by phase contrast. The setup significantly facilitates the production of section ribbons of vitreous samples This helps to collect a large number of sections, and the probability to have good ones among them is strongly increased. This will hopefully contribute to raising the usage of CEMOVIS

Sample preparation
Micromanipulators
Start of cryosectioning
Summary

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.